Curative

ABSTRACT

A coating created entirely from plant-derived ingredients is disclosed. Illustrative embodiments of the coating may be particularly well suited for use on leather-like materials created from epoxidized natural rubber-based formulations. Illustrative embodiments of the coating created may be comprised of substantially the reaction product between epoxidized vegetable oil and a polyfunctional naturally occurring acid (such as citric acid). Illustrative embodiments this reaction product may be used to produce porosity-free castable resins and vulcanize rubber formulations based on epoxidized natural rubber. Materials made from disclosed materials may be advantageously used as leather substitutes.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application claims priority from and is a continuation ofU.S. patent application Ser. No. 17/155,000 filed on Jan. 21, 2021,which is a continuation-in-part of U.S. patent application Ser. No.17/129,183 filed on Dec. 21, 2020 (now U.S. Pat. No. 11,407,856), whichapplication is a continuation of and claims priority from U.S.application Ser. No. 16/457,352 filed on Jun. 28, 2019 (now U.S. Pat.No. 10,882,950), which application claimed priority from and is acontinuation of U.S. application Ser. No. 16/388,693 filed on Apr. 18,2019 (now U.S. Pat. No. 10,400,061), which application claimed priorityfrom provisional U.S. App. Nos. 62/660,943 filed on Apr. 21, 2018;62/669,483 filed on May 10, 2018; 62/669,502 filed on May 10, 2018;62/756,062 filed on Nov. 5, 2018; 62/772,744 filed on Nov. 29, 2018;U.S. Pat. No. 62,772,715 filed on Nov. 29, 2018; and 62/806,480 filed onFeb. 15, 2019. U.S. patent application Ser. No. 17/155,000 filed on Jan.21, 2021, also claims priority from provisional Pat. App. Nos.62/963,325 filed on Jan. 20, 2020 and 63/084,508 filed on Sep. 28, 2020,all of which applications are incorporated by reference herein in theirentireties.

FIELD OF THE INVENTION

The present disclosure related to methods for producing natural productsthat may be made utilizing the curative disclosed herein. The naturalproducts have physical properties similar to synthetic coated fabrics,leather-based products, and foam products.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

No federal funds were used to develop or create the invention disclosedand described in the patent application.

BACKGROUND

The replacement of synthetic polymeric materials with naturally derivedand biodegradable polymers is an important goal in achieving sustainableproducts and material processes. Among all potential natural startingmaterials, those that are most prevalent in nature and easily captured,separated, and purified are also the most cost-effective replacementoptions. Materials such as wood, natural fibers, natural oils, and othernatural chemicals are all readily available in bountiful amounts.Heretofore, the limitations in using natural materials more broadly aredue primarily to limitations in processing flexibility (e.g.moldability) and/or ultimate properties (e.g. strength, elongation,modulus).

Natural animal-hide leather is a versatile material for which there arefew synthetic alternatives that meet the same performance attributes.Natural animal-hide leather in particular has a unique blend offlexibility, puncture resistance, abrasion resistance, formability,breathability, and imprintability. Synthetic leather substitutematerials are known in the art. Many utilize a fabric backing and apolyurethane or plasticized polyvinyl chloride elastomeric surface—suchmaterial constructions may achieve certain performance attributes ofnatural animal-hide leather but are not all-natural and are notbiodegradable. It is desirable to have a different material thatcomprises all-natural materials or at least contains a substantialportion of all-natural content. Furthermore, it is desirable that anyleather substitute be biodegradable to avoid disposal concerns.

Memory foam materials are entirely made of synthetic polymers today. Forexample, most commercial memory foam comprises polyurethane elastomerthat utilizes foam structure. Memory foam materials are characterized bylossy behavior, i.e. the polymer has a high loss modulus (tan δ). Memoryfoam materials are generally very stiff at temperatures substantiallybelow room temperature (e.g. below 10° C.), rubbery at temperaturessubstantially above room temperature (e.g. above 50° C.), andleather/lossy at or near room temperature (e.g. 15° C.-30° C.).

Liu (U.S. Pat. No. 9,765,182) discloses an elastomeric productcomprising epoxidized vegetable oil and a polyfunctional carboxylicacid. Because such ingredients are not miscible in each other, Liudiscloses the use of an alcohol solvent that is capable of solubilizingthe polyfunctional carboxylic acid and that is miscible with theepoxidized vegetable oil. An exemplary epoxidized vegetable oildisclosed by Liu is epoxidized soybean oil. An exemplary polyfunctionalcarboxylic acid disclosed by Liu is citric acid. Exemplary alcohols usedas a solubilizing agent include ethanol, butanol, and isopropyl alcohol.Liu discloses the creation of an elastomer by dissolving citric acid inethanol and then adding the entire amount of epoxidized soybean oil tothe solution. The solution is then heated to 50° C.-80° C. for 24 hrs toremove the ethanol (assisted by vacuum). Liu discloses that the optimaltemperature range for polymerization occurred at 70° C. (without anycatalysts). The Liu disclosure is clear that the evaporation temperaturerange for the alcohol solvent and polymerization temperature areoverlapping and thus there exhibits a high risk of prematurely curingthe polymer, i.e. forming a gel, before the entirety of the solvent isremoved. We have found that elastomers prepared by the method disclosedby Liu contain substantial porosity due to the evaporation of residualalcohol solvent after the onset of polymerization.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute apart of this specification, illustrate embodiments and together with thedescription, serve to explain the principles of the methods and systems.

FIG. 1 is a chemical reaction formula and schematic for at least oneillustrative embodiment of the curative disclosed herein.

FIG. 2A is an illustration of an epoxidized natural rubber-basedmaterial produced using a relatively lower viscosity resin that wasallowed to penetrate throughout the flannel substrate resulting in asuede or brushed-looking surface.

FIG. 2B is an illustration of an epoxidized natural rubber-basedmaterial produced using a relatively higher viscosity resin that wasallowed to only penetrate partly through the flannel substrate resultingin a glossy polished-looking surface.

FIG. 3 is an image of an epoxidized natural rubber-based materialproduced in accordance with the present disclosure.

FIGS. 4A, 4B, and 4C are views of portion of an epoxidized naturalrubber-based material produced in accordance with the present disclosurethat may be used for construction of wallet wherein each version of theepoxidized natural rubber-based material is made with a differenttexture.

FIG. 5 is a view of a plurality of pieces of a epoxidized naturalrubber-based material produced in accordance with the present disclosurethat may be used for construction of wallet.

FIG. 6 is a view of the plurality of pieces of the epoxidized naturalrubber-based material produced in accordance with the present disclosureassembled as a simple credit card wallet or carrier having theappearance, rigidity and strength as one of ordinary skill would expectwith natural animal-hide leather.

FIG. 7 is a resin impregnated fabric that may be utilized in accordancewith the present disclosure.

FIG. 8A is a top view of a ball made according to the presentdisclosure.

FIG. 8B is a side view of a ball made according to the presentdisclosure.

FIG. 9 provides a graphical representation for two stress-strain curvesof two different ENR-based materials.

FIG. 10A provides a depiction of an ENR-based material configured withinherent functionality for engaging a belt buckle.

FIG. 10B provides a depiction of the ENR-based material from FIG. 10Aafter engagement with a belt buckle.

FIG. 11 provides a depiction of an ENR-based material having grooves andridges formed therein.

FIG. 12 provides a depiction of an illustrative embodiment of a moldingsystem that may be used for certain ENR-based materials.

FIG. 13 shows pancake-like discs of foam product produced according toone embodiment of the present disclosure.

FIG. 14 shows a gradient of porosity associated with variation in curingtemperature.

DETAILED DESCRIPTION

Before the present methods and apparatuses are disclosed and described,it is to be understood that the methods and apparatuses are not limitedto specific methods, specific components, or to particularimplementations. It is also to be understood that the terminology usedherein is for the purpose of describing particular embodiments/aspectsonly and is not intended to be limiting.

As used in the specification and the appended claims, the singular forms“a,” “an,” and “the” include plural referents unless the context clearlydictates otherwise. Ranges may be expressed herein as from “about” oneparticular value, and/or to “about” another particular value. When sucha range is expressed, another embodiment includes from the oneparticular value and/or to the other particular value. Similarly, whenvalues are expressed as approximations, by use of the antecedent“about,” it will be understood that the particular value forms anotherembodiment. It will be further understood that the endpoints of each ofthe ranges are significant both in relation to the other endpoint, andindependently of the other endpoint.

“Optional” or “optionally” means that the subsequently described eventor circumstance may or may not occur, and that the description includesinstances where said event or circumstance occurs and instances where itdoes not.

“Aspect” when referring to a method, apparatus, and/or component thereofdoes not mean that limitation, functionality, component etc. referred toas an aspect is required, but rather that it is one part of a particularillustrative disclosure and not limiting to the scope of the method,apparatus, and/or component thereof unless so indicated in the followingclaims.

Throughout the description and claims of this specification, the word“comprise” and variations of the word, such as “comprising” and“comprises,” means “including but not limited to,” and is not intendedto exclude, for example, other components, integers or steps.“Exemplary” means “an example of” and is not intended to convey anindication of a preferred or ideal embodiment. “Such as” is not used ina restrictive sense, but for explanatory purposes.

Disclosed are components that can be used to perform the disclosedmethods and apparatuses. These and other components are disclosedherein, and it is understood that when combinations, subsets,interactions, groups, etc. of these components are disclosed that whilespecific reference of each various individual and collectivecombinations and permutation of these may not be explicitly disclosed,each is specifically contemplated and described herein, for all methodsand apparatuses. This applies to all aspects of this applicationincluding, but not limited to, steps in disclosed methods. Thus, ifthere are a variety of additional steps that can be performed it isunderstood that each of these additional steps can be performed with anyspecific embodiment or combination of embodiments of the disclosedmethods.

The present methods and apparatuses may be understood more readily byreference to the following detailed description of preferred aspects andthe examples included therein and to the Figures and their previous andfollowing description. Corresponding terms may be used interchangeablywhen referring to generalities of configuration and/or correspondingcomponents, aspects, features, functionality, methods and/or materialsof construction, etc. those terms.

It is to be understood that the disclosure is not limited in itsapplication to the details of construction and the arrangements ofcomponents set forth in the following description or illustrated in thedrawings. The present disclosure is capable of other embodiments and ofbeing practiced or of being carried out in various ways. Also, it is tobe understood that phraseology and terminology used herein withreference to device or element orientation (such as, for example, termslike “front”, “back”, “up”, “down”, “top”, “bottom”, and the like) areonly used to simplify description, and do not alone indicate or implythat the device or element referred to must have a particularorientation. In addition, terms such as “first”, “second”, and “third”are used herein and in the appended claims for purposes of descriptionand are not intended to indicate or imply relative importance orsignificance.

Element Description Element Number Natural leather-like material (suedefinish) 100 Natural leather-like material (glossy finish)  100′ Fabric102 Fabric extension 103 Polymer 104

1. Curative (Pre-Polymer)

Disclosed is a curative comprised of an epoxidized triglyceride (whichmay be a plant-based oil such as vegetable and/or nut oil(s) and/or amicrobial oil such as that produced by algae or yeast), naturallyoccurring polyfunctional carboxylic acids, and at least some graftedhydroxyl-containing solvent. Examples of such epoxidized triglyceridescomprised of plant-based oils include epoxidized soybean oil (ESO),epoxidized linseed oil (ELO), epoxidized corn oil, epoxidized cottonseedoil, epoxidized canola oil, epoxidized rapeseed oil, epoxidized grapeseed oil, epoxidized poppy seed oil, epoxidized tongue oil, epoxidizedsunflower oil, epoxidized safflower oil, epoxidized wheat germ oil,epoxidized walnut oil, and other epoxidized vegetable oils (EVOs).Generally, any polyunsaturated triglyceride with an iodine number of 100or greater may be epoxidized and used with the curative as disclosedherein without limitation unless otherwise indicated in the followingclaims. Such epoxidized triglycerides are generally known to bebiodegradable. Examples of naturally occurring polyfunctional acidsinclude citric acid, tartaric acid, succinic acid, malic acid, maleicacid, and fumaric acid. Although specific illustrative embodiments maydenote one type of oil and/or acid, such embodiments are not meant to belimiting in any way unless otherwise indicated in the following claims.

The curative as disclosed herein is a reaction product between anepoxidized vegetable oil(s) and a naturally occurring polyfunctionalcarboxylic acid conducted in a solvent that is capable of solubilizingboth the epoxidized vegetable oil(s) and a naturally occurringpolyfunctional carboxylic acid, wherein the solvent contains at leastsome portion of a hydroxyl-containing solvent (i.e., an alcohol) thatreacts with at least some portion of the carboxylic acid functionalgroups that are contained on the polyfunctional carboxylic acid. Thecurative is an oligomeric structure of carboxylic-acid-capped epoxidizedvegetable oil, heretofore called a pre-polymer curative. The curative isa viscous liquid that is soluble in unmodified epoxidized vegetable oiland other epoxidized plant-sourced polymers (e.g., epoxidized naturalrubber).

Generally the terms “curative,” “pre-polymer,” and “pre-polymercurative” are used to denote the same and/or similar chemical structureas disclosed in this Section 1. However, the function of the curative,pre-polymer, and pre-polymer curative may be different in differentapplications thereof to produce different end products. For example,when the curative is used with epoxy-containing monomeric resins (e.g.,EVOs) it functions to build molecular weight that is integral to thebackbone of the resultant polymer and therefore may be referred to as apre-polymer in such applications. In another example, when the curativeis used in applications having pre-existing high molecular weightepoxy-containing polymer (e.g., as disclosed below herein) the curativeis functioning primarily to link those pre-existing high molecularweight polymers and therefore may be referred to simply as a curative insuch applications. Finally, when the curative is used in applicationshaving both substantial amounts of epoxy-containing monomer and someportion of pre-existing high molecular weight epoxy-containing polymerit functions both to build molecular weight and to link pre-existinghigh molecular weight polymers and therefore may be referred to as apre-polymer curative.

It has been found that the creation of a curative can eliminate the riskof porosity due to solvent evaporation during the curing process.Furthermore, the oligomeric curative may incorporate substantially allof the polyfunctional carboxylic acid so that no additional curative isrequired during the curing process. For example, citric acid is notmiscible in epoxidized soybean oil (ESO) but they may be made to reactwith each other in a suitable solvent. The amount of citric acid may beselected so that the curative is created so that substantially all ofthe epoxide groups of the ESO in the curative are reacted withcarboxylic acid groups of the citric acid. With sufficiently excesscitric acid, the pre-polymerization extent may be limited so that no gelfraction is formed. That is, the target species of the curative is a lowmolecular weight (oligomeric) citric-acid capped ester-product formed bythe reaction between carboxylic acid groups on the citric acid withepoxide groups on the ESO. The solvent used for the reaction mediumcontains at least some portion of a hydroxyl-containing solvent (i.e.,an alcohol) that is grafted unto at least some of the polyfunctionalcarboxylic acid during the creation of the curative. Although specificillustrative embodiments may denote one type of alcohol (e.g., IPA,ethanol, etc.), such embodiments are not meant to be limiting in any wayunless otherwise indicated in the following claims.

Illustrative oligomeric curatives may be created with weight ratios ofESO to citric acid in the range of 1.5:1-0.5:1, which corresponds to amolar ratio of epoxide groups:carboxylic acid groups of approximately0.43:1 (for a weight ratio of 1.5:1) to 0.14:1 (for the weight ratio of0.5:1). In on illustrative embodiment a weight ratio of ESO:citric acidis 1:1, which gives a molar ratio of epoxide groups:carboxylic acidgroups of 0.29:1. If too much ESO is added during curative creation, thesolution may gel and further incorporation of ESO to create the targetresin becomes impossible. Note that on a weight basis, stoichiometricequivalent amounts of epoxide groups on the ESO (molecular weight of˜1000 g/mol, functionality of 4.5 epoxide groups per molecule) andcarboxylic acid groups on the citric acid (molecular weight 192 g/mol,functionality of 3 carboxylic groups per molecule) occur at a weightratio of 100 parts of ESO to about 30 parts of citric acid. A weightratio of ESO:citric acid above 1.5:1 may build a curative with excessivemolecular weight (and hence viscosity) which limits its ability to beincorporated into unmodified epoxidized vegetable oil or epoxidizednatural rubber. If the weight ratio of ESO:citric acid is below 0.5:1 ithas been found that there is so much excess citric acid that aftersolvent evaporation, ungrafted citric acid may precipitate out ofsolution.

In addition to controlling the ratio of ESO to citric acid, throughexperimentation it has been found that selective control of the amountof alcohol used as a solvent may also be used to tailor the physicalproperties of the resulting elastomer made with the curative. Thealcohol solvent itself is incorporated into the elastomer by formingester linkages with the polyfunctional carboxylic acid. A mixture of twoor more solvents may be used to tailor the amount of grafting of ahydroxyl-containing solvent onto the citric acid-capped oligomericcurative. A schematic depiction of the chemical reaction for making anillustrative embodiment of the curative disclosed herein is shown inFIG. 1 .

For example, and without restriction or limitation, isopropyl alcohol(IPA), ethanol, or other suitable alcohol without limitation unlessotherwise indicated in the following claims may be used as a componentof a solvent system used to miscibilize citric acid with ESO. IPA,ethanol, or other suitable alcohol are capable of forming an esterlinkage via a condensation reaction with citric acid. Since citric acidhas three carboxylic acids, such grafting reduces the averagefunctionality of the citric acid molecules that are reacting with theESO. This is beneficial in creating an oligomeric structure that is morelinear and therefore less highly branched. Acetone may be used as onecomponent of a solvent system used to miscibilize citric acid with ESO,but unlike IPA or ethanol, acetone itself is not capable of beinggrafted onto the citric acid-capped oligomeric curative. Indeed, duringcreation of the oligomeric curative it has been found that thereactivity of the pre-polymer is determined, in part, by the ratio ofthe alcohol to acetone that may be used to solubilize citric acid withESO. That is, in reaction mixtures with the similar amounts of citricacid and ESO, a curative created from a solution with a relatively highratio of alcohol to acetone creates a curative with longer,less-highly-branched structures than curative created from a solutionwith a relatively low ratio of alcohol to acetone under similar reactionconditions.

Generally, a curative may be adapted for use with additional unmodifiedepoxidized vegetable oil to yield a castable resin. The improvedmethodology disclosed by Applicant herein results in substantiallyporosity-free elastomeric products.

2. Coated Materials

A. Summary

The curative as disclosed immediately above may function as apre-polymer and may be mixed with additional epoxidized vegetable oil tobe used as a resin which may be applied to various backingmaterials/backing layers to yield a leather-like material with excellenttear strength, flexibility, dimensional stability, and fabricationintegrity. Throughout this disclosure, the terms “backing material” and“backing layer” may be used interchangeably depending the specificcontext. However, for certain articles disclosed herein a backingmaterial may be comprised of a resin-impregnated backing layer.According to one illustrative embodiment of a coated material utilizingthe pre-polymer, one illustrative fabric backing material/backing layermay be a woven cotton flannel (as depicted in FIGS. 2A & 2B anddescribed in more detail below). If the resin is formulated to berelatively low in viscosity, exposed flannel may persist above theresin-coated fabric core. This imparts a warm texture to the surface ofthe article. Other fabric backing material/backing layer may includewoven substrates of various kinds (e.g., plain weave, twill, sateenweave, denim), knitted substrates, and non-woven substrates withoutlimitation unless indicted in the following claims.

In other embodiments, the resin may be coated onto a non-stick surface(e.g., silicone or PTFE) or texture paper at a consistent layerthickness. After the film has been coated to an even layer, a layer ofbacking material may be laid on top of the liquid resin. The liquidresin may wick into the fabric layer (i.e., backing material) creating apermanent bond with the fabric during curing. The article may then beplaced in an oven to complete the cure of the resin. Temperatures forcuring may be preferably 60° C.-100° C., or even more preferably 70°C.-90° C. for a duration of 4 hr-24 hr. Longer cure times are alsopermissible. Alternatively, the liquid resin may be applied onto anon-stick surface (e.g., silicone or PTFE) or texture paper at aconsistent layer thickness after which fabric may be laid on top of theliquid resin and then another non-stick surface may be laid on top ofthe resin and fabric. This assembly may be placed in a heated moldingpress to complete the cure. Cure temperatures within a press mayoptionally be higher than in an oven because the molding pressureminimizes the creation of bubbles (voids) in the final article. Curetemperatures within a press may be between 80° C.-170° C., or even morepreferably, 100° C.-150° C. for a duration of 5 minutes-60 minutes, ormore preferably between 15 minutes-45 minutes.

The resin may be optically clear with a slight yellow hue. Resin thathas no pigment added may be used to create oil-cloth like materials thatallow for fabrics to be made water resistant and wind resistant whilestill allowing the fabric patterns to be visible within the resin.Coated fabrics made according to this embodiment may be cured either inan oven (without press molding) or may be cured within a heated press.Such coated fabrics may be used for garments, particularly forouterwear, or for waterproof accessories; including, but not limited to,purses, handbags, backpacks, duffle bags, luggage, briefcases, hats, andthe like.

Novel embossed items have been created using the resin described in thisdisclosure in combination with non-woven mats comprised of virgin orrecycled textile fibers. Specifically, non-woven webs from about 7 mmthick to about 20 mm thick may be impregnated by resins preparedaccording to this disclosure. After impregnation, the non-woven webs maybe pressed in a heated hydraulic press to a nominal pressure of between10 psi-250 psi, or even more preferably between 25 psi-100 psi. Thenon-woven web with resin may be pressed between silicone release liners,one of which may have an embossing pattern therein. The embossingpattern may have relief characteristics of a depth between 1 mm-6 mm, ormore preferably between 2 mm and 4 mm in depth. When resin preparedaccording to this disclosure is further pigmented with a structuralcolor pigment, e.g., mica pigments of various shades—many of which havepearlescent qualities—and such resin is molded into a non-woven web withan embossing pattern, it has been found to create aesthetically pleasingpatterned articles. The structural color has been found topreferentially align at embossing features to create sharp contrasts andvisual depth corresponding to the embossed pattern. Alternatively, andwithout restriction unless so indicated in the following claims, mineralpigments from other source rocks and processes may be included in thecasting resin to impart color to articles made according to the presentdisclosure.

Resin coated fabrics made also be created according to one embodiment ofthe present disclosure using roll-to-roll processing. In a roll-to-rollprocess of textured, coated fabrics, including leather-like materials,the texture paper is often used as a carrier film to move both the resinand the fabric through an oven for a specific duration of time. Theresin according to the present disclosure may require cure times thatare longer than PVC or polyurethane resins that are currently used inthe art, thus the line speeds may be correspondingly slower or the cureovens may be made longer to effect a longer cure time. Vacuum degassingof the resin prior to casting may allow for higher temperatures to beused for curing (due to less residual solvent, moisture, and trappedair) that would speed up the cure time and thus the line pull rate.

Alternatively, certain catalysts are known in the art to speed up thecarboxylic acid addition to epoxide groups. Base catalysts may be addedto the resin; some example catalysts include pyridine, isoquinoline,quinoline, N,N-dimethylcyclohexylamine, tributylamine,N-ethylmorpholine, dimethylaniline, tetrabutyl ammonium hydroxide, andsimilar molecules. Other quaternary ammonium and phosphonium moleculesare known catalysts for the carboxylic acid addition to epoxide groups.Various imidazoles are likewise known as catalysts for this reaction.Zinc salts of organic acids are known to improve the cure rate as wellas impart beneficial properties, including improved moisture resistance,to the cured films. (See Werner J. Blank, Z. A. He and Marie Picci,“Catalysis of the Epoxy-Carboxyl Reaction”, Presented at theInternational Waterborne, High-Solids and Powder Coatings Symposium,Feb. 21-23, 2001.) Accordingly, any suitable catalyst may be usedwithout limitation unless otherwise indicated in the following claims.

B. Illustrative Embodiments

Although the illustrative embodiments and methods that follow includespecific reaction parameters (e.g., temperatures, pressures, reagentratios, etc.), those embodiments and methods are for illustrativepurposes only and in no way limit the scope of the present disclosureunless otherwise indicated in the following claims.

First Illustrative Embodiment and Method

To make a first illustrative embodiment of a coated material using thepre-polymer (that is, the curative as disclosed previously above), 18parts of citric acid were dissolved into 54 parts of warm IPA. To thissolution, only 12 parts of ESO is added. The IPA was evaporated withcontinuous heating and stirring (above ˜85° C.). This was found to makea viscous liquid that could be heated to above 120° C. without gelation(even for long periods of time). This viscous liquid pre-polymer wasallowed to cool below 80° C. To this viscous liquid, 88 parts of ESO isadded. The final liquid resin will polymerize to a solid elastomericproduct in 1-5 minutes at ˜150° C. The coated material (which may serveas a substitute for natural animal-hide leather) may be formed as areaction product using an epoxidized triglyceride and the pre-polymerwithout limitation unless otherwise indicated in the following claims.

Second Illustrative Embodiment and Method

For this illustrative embodiment, 30 parts of citric acid were dissolvedinto 60 parts of warm IPA. To this solution, 20 parts of ESO were slowlyadded while stifling. The IPA was evaporated with continuous heating andstirring (above 85° C., and preferably above 100° C.). This viscouspre-polymer was allowed to cool below 80° C. (preferably below 70° C.)and 80 parts of ESO were added along with various structural colorpigments and 0.5 parts of zinc stearate (as an internal mold releaseagent). The resulting resin was poured over cellulosic fabric andallowed to cure at ˜120° C. for 10-30 minutes. After initial cure, thematerial was placed in an 80° C. oven for overnight post-curing (˜16hours). The surface of the material was then sanded smooth (andoptionally polished). The resulting material was found to haveleather-like attributes.

Third Illustrative Embodiment and Method

Pre-polymer creation has been conducted by dissolving 50 parts of citricacid in 100 parts of warm IPA, accelerated by mixing. After dissolutionof the citric acid, 50 parts of ESO is added to the stirring solution.The mixture is kept on a hot plate while the IPA evaporated undercontinuous heat and stirring. Such solutions have been created multipletimes with various hot plate temperatures and air flow conditions. Evenafter extended times of heating and stirring, it has repeatedly beenfound that the amount of reaction product is greater than the mass ofthe ESO and citric acid alone. Depending on the rate of IPA evaporation(determined at least by air flow, mixing rate, and hot platetemperature) between 2.5 and 20 parts of the IPA has been found to begrafted onto the citric-acid capped oligomeric pre-polymer. Furthermore,solvent blends of acetone and IPA may be used as the reaction mediumwherein the ratio between acetone and IPA determines the amount ofresidual carboxylic acid functional groups on the pre-polymer as well asthe amount of branching in the pre-polymer. Higher amounts of IPA createmore linear structures by lowering the effective functionality of thecitric acid by capping some of the carboxylic acid functional groups bygrafting IPA unto the citric acid via an ester linkage as referenced inFIG. 1 . Lower amounts of IPA create more highly branched structureswith more residual carboxylic acid functional groups.

Fourth Illustrative Embodiment and Method

Pre-polymer creation has been conducted by dissolving 50 parts of citricacid in 100 parts of warm IPA, accelerated by mixing. After dissolutionof the citric acid, 50 parts of ESO and 15 parts of dewaxed blondeshellac is added to the stirring solution. The mixture is kept on a hotplate the while IPA evaporated under continuous heat and stirring. Theshellac was found to increase the viscosity of the resultingpre-polymer.

Fifth Illustrative Embodiment and Method

Pre-polymer creation has been conducted by dissolving 45 parts of citricacid in 90 parts of warm IPA, accelerated by mixing. After dissolutionof the citric acid, 45 parts of ESO is added to the stirring solution.The mixture is kept on a hot plate while the IPA evaporated undercontinuous heat and stirring.

Sixth Illustrative Embodiment and Method

Pre-polymer creation has been conducted by dissolving 45 parts of citricacid in 30 parts of warm IPA and 60 parts of acetone, accelerated bymixing. After dissolution of the citric acid, 45 parts of ESO is addedto the stirring solution. The mixture is kept on a hot plate while theacetone and IPA evaporated under continuous heat and stirring. Suchsolutions have been created multiple times with various hot platetemperatures and air flow conditions. Even after extended times ofheating and stirring, it has repeatedly been found that the amount ofreaction product is greater than the mass of the ESO and citric acidalone, but the amount of grafted IPA is less than in pre-polymer createdaccording to the fifth illustrative embodiment (even though the ratio ofESO:citric acid is 1:1 in both cases). Furthermore, pre-polymer createdaccording to the fifth illustrative embodiment is lower in viscositycompared to pre-polymer created according to the sixth illustrativeembodiment.

Generally, it is contemplated that the greater content of IPA during thepre-polymer creation allowed more IPA to be grafted onto carboxylic-acidsites on the citric acid, thus lowering the average functionality of thecitric acid and thus creating a less highly branched oligomericpre-polymer. In no circumstance have reaction conditions been found thatcapping of the citric acid with IPA to such an extent that final curingof the resin is prohibited.

Seventh Illustrative Embodiment and Method

The pre-polymer created in the fourth illustrative embodiment was mixedwith additional ESO to bring the total calculated amount of ESO to 100parts. This mixture was found to cure into a transparent, elastomericresin. Tensile testing according to ASTM D412 found that the tensilestrength was 1.0 MPa with an elongation at break of 116%.

Eight Illustrative Embodiment and Method

Pre-polymer was created by dissolving 45 parts of citric acid in 20parts of IPA and 80 parts of acetone under heating and stirring. Afterdissolution of the citric acid, 35 parts of ESO was added to thesolution along with 10 parts of shellac. The pre-polymer created afterevaporation of the solvents was then cooled. The pre-polymer was mixedwith an additional 65 parts of ESO to bring the total amount of ESO to100 parts. The mixed resin was then cast on a silicone mat to make atransparent sheet. The mechanical properties of the material were foundby tensile testing according to ASTM D412. The tensile strength wasfound to be 1.0 MPa and the elongation was 104%, which gives acalculated modulus of 0.96 MPa.

Ninth Illustrative Embodiment and Method

Pre-polymer was created by dissolving 45 parts of citric acid in 5 partsof IPA and 80 parts of acetone under heating and stifling. Afterdissolution of the citric acid, 35 parts of ESO was added to thesolution along with 10 parts of shellac. The pre-polymer created afterevaporation of the solvents was then cooled. The pre-polymer was mixedwith an additional 65 parts of ESO to bring the total amount of ESO to100 parts. The mixed resin was then cast on a silicone mat to make atransparent sheet. The mechanical properties of the material were foundby tensile testing according to ASTM D412. The tensile strength wasfound to be 1.8 MPa and the elongation was 62%, which gives a calculatedmodulus of 2.9 MPa. As can be seen from the eighth and ninthillustrative embodiments, the lower amount of IPA present duringpre-polymer creation yields a pre-polymer that creates a more highlycrosslinked resin with higher modulus and lower elongation. Thesereaction products are more plastic-like and less rubber-like in theirmaterial attributes.

Tenth Illustrative Embodiment and Method

Pre-polymer was created by dissolving 25 parts of citric acid in 10parts of IPA and 80 parts of acetone under heating and stirring. Afterdissolution of the citric acid, 20 parts of ESO was added to thesolution along with 5 parts of shellac. The pre-polymer created afterevaporation of the solvents was then cooled. The pre-polymer was mixedwith an additional 80 parts of ESO to bring the total amount of ESO to100 parts. The mixed resin was then cast on a silicone mat to make atransparent sheet. The mechanical properties of the material were foundby tensile testing according to ASTM D412. The tensile strength wasfound to be 11.3 MPa and the elongation was 33%, which gives acalculated modulus of 34 MPa. As can be seen from the tenth illustrativeembodiment, by appropriate design of the pre-polymer and the final resinmixture, a plastic material with the attributes of high strength andhigh modulus may be created by the methods of the present disclosure.

Eleventh Illustrative Embodiment and Method

The pre-polymer of the sixth illustrative embodiment was mixed withadditional ESO to bring the total calculated amount of ESO to 100 parts.The mixed resin was then cast on a silicone mat to make a transparentsheet. The mechanical properties of the material were found by tensiletesting according to ASTM D412. The tensile strength was found to be 0.4MPa and the elongation was 145%, which gives a calculated modulus of0.28 MPa.

As can be seen from the eleventh illustrative embodiment, by appropriatedesign of the pre-polymer and the final resin mixture, a high elongationelastomeric material by be created by the methods of the presentdisclosure. Therefore, by appropriate design of the pre-polymer, theinventive methods may be used to produce materials ranging from stiff,plastic-like materials to high-elongation elastomeric materials.Generally, higher amounts of IPA grafted during pre-polymer formationlowers the stiffness of the resulting material. Higher amounts ofdissolved shellac yield stronger materials with somewhat higherstiffness. Citric acid amount (relative to the final mixed recipe) maybe used either above stoichiometric balance or below to lower themodulus. Citric acid amounts near stoichiometric balance (˜30 parts byweight to 100 parts by weight ESO) generally yield the stiffestmaterials; unless offset by high levels IPA grafting of the carboxylicacid groups during pre-polymer formation.

One of the beneficial attributes of animal-based leather is itsflexibility over a wide range of temperatures. Synthetic-polymer basedleather substitutes based on PVC or polyurethane may become particularlystiff at temperatures below −10° C. or below −20° C. (based on testingaccording to CFFA-6a—Cold Crack Resistance—Roller method). Materialsprepared according to some of the embodiments of the present disclosuremay have poor cold crack resistance. In the following examples,formulations are given that improve cold crack resistance. Cold crackresistance may be improved by adding a flexible plasticizer. Somenatural vegetable oils may exhibit good low temperature flow, especiallypreferred may be polyunsaturated oils. Such oils may be anynon-epoxidized triglycerides (such as those disclosed in Section 1above) having relatively high iodine numbers (e.g., greater than 100)without limitation unless otherwise indicated in the following claims.Alternatively, monounsaturated oils may be added as plasticizers; oneillustrative oil may be castor oil which is found to be thermally stableand less prone to becoming rancid. Additionally, the fatty acids andfatty acid salts of these oils may be used as a plasticizer.Accordingly, the scope of the present disclosure is in no way limited bythe presence of or particular chemistry of a plasticizer unlessotherwise indicated in the following claims.

Another approach is to use a polymeric additive that may impart improvedlow temperature flexibility. A preferred polymeric additive may beEpoxidized Natural Rubber (ENR). ENR is available commercially indifferent grades with various levels of epoxidation, for example 25%epoxidation of the double bonds yields grade ENR-25, 50% epoxidation ofthe double bonds yields grade ENR-50. Higher levels of epoxidationincrease the glass transition temperature, T_(g). It is advantageous forthe T_(g) to remain as low as possible for the most improvement in coldcrack resistance in the final resin, so ENR-25 may be the preferredgrade for use as a polymeric plasticizer. Even lower levels ofepoxidation may be advantageous for further lowering of the cold cracktemperature in the final resin. However, the scope of the presentdisclosure is not so limited unless otherwise indicated in the followingclaims.

Twelfth Illustrative Embodiment and Method

ENR-25 was mixed with ESO on a two-roll rubber compounding mill. It wasfound that ESO could slowly be added until a total of 50 parts of ESOcould be added to 100 parts of ENR-25 before the viscosity dropped sofar that further mill mixing was impossible. This gooey material wasthen transferred to containers for further mixing in a Flacktek®Speedmixer. A flowable mixture was achieved when a total of 300 parts ofESO was finally incorporated into 100 parts of ENR-25. The mixturecreated did not phase segregate.

The material of the twelfth illustrative embodiment may be mixed in asingle step by a number of means known in the art, without restrictionor limitation unless indicated in the following claims. Specifically,so-called Sigma Blade mixers may be used to create a homogenous mixtureof ENR and ESO in a single step. Likewise, a kneader, such as a BlissKneader, by used to create such mixtures in a continuous mixer-typearrangement which is well known to one of ordinary skill in the art. Thehomogeneous mixture may be mixed with pre-polymers as described in priorexamples to create a spreadable resin that may be used as a leather-likematerial with improved cold crack resistance. Additionally, materialscreated with ENR-modified ESO as disclosed by the twelfth illustrativeembodiment may exhibit improved tear strength, elongation, and abrasionresistance when compared to resins that do not contain ENR.

C. Additional Treatments

Articles produced according to this disclosure may be finished by anymeans known in the art. Such means include, but are not limited to,embossing, branding, sanding, abrading, polishing, calendering,varnishing, waxing, dyeing, pigmenting, and the like unless otherwiseindicated in the following claims. Exemplary results may be obtained byimpregnating the resin of the present disclosure onto fabric or anon-woven mat and curing such article. After curing the article, thesurfaces may be sanded to remove imperfections and expose some portionof the substrate. Such surfaces exhibit characteristics very analogousto animal-hide leather, as exemplified by FIGS. 3-7 . The surfaces thenmay be treated with natural oil or wax protectants, subject to aparticular application.

D. Applications/Illustrative Products

Coated fabrics, ENR-based materials, and/or oil cloth-like materialsproduced according to the present disclosure may be used in applicationswhere animal-hide leather and/or synthetic resin-coated fabrics are usedtoday. Such applications may include belts, purses, backpacks, shoes,table tops, seating, and the like without limitation unless otherwiseindicated in the following claims. Many of these articles are consumableitems that if made from synthetic material alternatives arenon-biodegradable and are non-recyclable. If such items are instead madeaccording to the present disclosure, they would be biodegradable andthus not create a disposal problem as the biodegrability of similarlyprepared polymers made from ESO and natural acids has been studied andshown. Shogren et al., Journal of Polymers and the Environment, Vol. 12,No. 3, July 2004. Furthermore, unlike animal-hide leather, whichrequires significant processing to be made durable and stable (some ofwhich uses toxic chemicals), the materials disclosed herein may requireless processing and will use environmentally friendly chemicals.Additionally, animal-hide leather is limited in size and may containdefects that render large pieces inefficient to produce. The materialdisclosed herein does not have the same kind of size limitations.

A cross-sectional depiction of the resulting material when a liquidresin precursor such as those described for various illustrativeembodiments and methods above was applied to cotton flannel fabric thatwas placed over a heated surface (a hot plate) is shown in FIGS. 2A &2B. The resin was found to react in 1-5 minutes when the surfacetemperature of the hot plate was ˜130° C.-150° C. The viscosity of theresin may be controlled by the time allowed for polymerization prior topouring over the surface. By controlling the viscosity, the degree ofpenetration into the surface may be controlled to achieve variouseffects in the resultant product. For example, a lower viscosity resinmay penetrate throughout the fabric 102 and leave a suede orbrushed-looking surface as shown in FIG. 2A to create a naturalleather-like material 100 having a suede finish. A higher viscosityresin may penetrate only partly through the fabric 102 and result in aglossy, polished-looking surface as shown in FIG. 2B to create a naturalleather-like material 100′ having a glossy finish. In this way,variations may be created that mimic natural animal-hide leatherproducts. As shown in contrasting FIGS. 2A & 2B, the naturalleather-like material 100 having a suede finish 100 may exhibit a largernumber of fabric extensions 103 extending from the fabric 102 throughthe polymer 104 than does the natural leather-like material 100′ havinga glossy finish. In the natural leather-like material 100′ having aglossy finish, the majority of fabric extensions 103 may terminatewithin the polymer 104.

Alternatively, an article with a suede-like (i.e., relatively soft)surface without resin may be created by embedding flannel in anon-miscible paste (e.g., silicone vacuum grease) that is coated on ahot plate. The resin can then be poured over the surface of the flannelbut will not penetrate through the non-miscible paste. After curing, thenon-miscible paste may be removed from the article leaving that surfacewith a suede-like feeling. One of ordinary skill will thereforeappreciate that a natural leather-like material as disclosed herein maybe produced as the reaction product between an epoxidized vegetable oiland a naturally occurring polyfunctional acid impregnated upon a cottonflannel substrate, without limitation or restriction, wherein thearticle thus formed has the reaction product impregnated only partlythrough the substrate with substantially unimpregnated flannel on oneside of the article. Although cotton flannel was used in these examples,any suitable flannel and/or fabric may be used including but not limitedto those made from linen, hemp, ramie, and other cellulosic fiberswithout limitation unless otherwise indicated in the following claims.Additionally, non-woven substrates may be used as well recycledsubstrates (upcycled). Brushed knits may be used to impart additionalstretch to the resultant article. Random mats (e.g., Pellon, also knownas batting) may be advantageously used as a substrate for certainarticles. In another illustrative embodiment, a textile backing layerand/or backing material may be configured from a protein-based fiber,which fibers include but are not limited to of wool, silk, alpaca fiber,qiviut, vicuna fiber, llama wool, cashmere, and angora unless otherwiseindicated in the following claims.

Additional illustrative products that may be made according to thepresent disclosure are shown in FIGS. 3-8B. A depiction of a sheet ofmaterial that may serve as a natural leather-like material is shown inFIG. 3 , and FIGS. 4-6 show various natural leather-like materials thatmay be used to construct a wallet. The material in FIGS. 4A, 4B, & 4C isshown with a plurality of apertures made therein, which apertures may bemade with a conventional drill without limitation unless otherwiseindicated in the following claims. Contrasting FIGS. 4A, 4B, & 4C showsthat the method for making the material may be configured to impart awide variety of textures thereon, which textures include but are notlimited to smooth, grainy, soft, etc. (e.g., similar to that of variousanimal-hide leathers) unless otherwise indicated in the followingclaims.

The material pieces shown in FIGS. 5 & 6 may be cut using a lasercutter. Unlike animal-hide leather, the laser cutting did not char ordegrade the edges of the natural leather-like material along thecutline. A finished wallet constructed of a natural leather-likematerial made according to the present disclosure is shown in FIG. 6 .The separate pieces shown in FIG. 5 may be conventionally assembled(e.g., sewn) to construct a simple credit card wallet or carrier (asshown in FIG. 6 ) having the appearance, rigidity, and strength as onewould expect in a similar article made from animal-hide leather. Thenatural leather-like material may be sewn and/or otherwise processedinto a finished product using conventional techniques without limitationunless otherwise indicated in the following claims. As shown in FIG. 7and as described in detail above, a fabric may be impregnated with aresin to provide various characteristics to an article made according tothe present disclosure.

Additionally, the resin produced according to the present disclosure maybe pigmented to match the coloration of natural animal-hide leather. Ofparticular utility are structural color pigments and/or mineral pigmentsthat do not contain any harmful substances. One such example ofillustrative structural color pigments is Jaquard PearlEx® pigments. Ithas been found that the blending of structural color pigments atrelatively low loadings creates a natural leather-like material that hasexcellent visual aesthetics. Another such illustrative example of asuitable pigment may be procured from Kreidezeit Naturfarben, GmbH.Furthermore, it has been found that lightly sanding the resultantsurface results in a material that strongly resembles tanned & dyedanimal-hide leather.

Although the examples disclosed utilized only one layer of fabric, otherillustrative samples have been created with multiple fabric layers tocreate thicker leather-like products. Since the reaction between epoxidegroups and carboxylic groups does not create any condensationby-products, there is no inherent limit to the cross-sectional thicknessthat may be created. Resin-coated fabrics and non-wovens are used inapplications such as office furniture, including seating, writingsurfaces, and room dividers; in garments, including jackets, shoes, andbelts; in accessory items, including handbags, purses, luggage, hats,and wallets; and may be useful in residential decorations, includingwallcoverings, floor coverings, furniture surfaces, and windowtreatments. Current applications that are served by animal-based leathermay be considered potential applications for materials made according tothe present disclosure.

Furthermore, current applications that are served by petrochemical-basedflexible films; notably those served by PVC and polyurethane-coatedfabrics, may be considered potential applications for materials madeaccording to the present disclosure. In addition, the resin as disclosedherein is substantially free of any off-gassing vapors when curedaccording to the times and temperatures as disclosed herein. Therefore,applications that are thicker than traditional films may also be servedby the resins prepared according to the present disclosure. For example,the resin may be used to cast three-dimensional items in suitable molds.A top view of such a three-dimensional item configured as a ball madeaccording to the present disclosure is provided in FIG. 8A, and a sideview thereof is shown in FIG. 8B. The ball may be resin-based and may beproduced from epoxidized soy oil and citric acid-based recipes alongwith structural color pigments. Simple tests indicate it has very lowrebound and is expected to have excellent vibration absorptionqualities.

Prior art three-dimensional cast resin items are typically made ofstyrene-extended polyester (orthophthallic or isophthalic systems). Suchitems may currently consist of two-part epoxies or two-part polyurethaneresins. Such items may currently consist of silicone casting resins. Oneexample of an application currently served by two-part epoxies is thethick-film coating of tables and decorative inlays, wherein the epoxymay be selectively pigmented to create a pleasing aesthetic design. Suchapplications have been successfully duplicated with casting resinscreated according to the present disclosure. Furthermore, small chesspieces have been successfully cast from resins created according to thepresent disclosure without detrimental off-gassing or trapped air.Accordingly, a wide array of applications exist for various materialsmade according to the present disclosure and the specific intended useof the final article produced by any method disclosed herein is notlimited to a particular application unless otherwise indicated in thefollowing claims.

E. Resinous Coatings, Products, and Methods

In various illustrative embodiments disclosed herein, natural productsmay have physical properties similar to synthetic coated fabrics,animal-based leather products, and foam products. As disclosed thephysical properties of the natural products may be further enhanced toimprove flexibility.

Background

Coatings are present on many consumer goods where such coatings areapplied to provide surface protection and/or coloration. In addition, insome consumer goods, the coating may serve primarily to improve thehaptics (that is, the tactile feel) of a surface. In one class ofmaterials, namely animal-based leather and leather-like materials,surface coatings may be provided to provide surface protection,coloration, and improved haptics. For animal-based leather, suchcoatings may be substantially absorbed into the substrate and complementthe natural haptics of the leather. Such coatings may be based on oils,waxes, and/or polymers (both natural and synthetic). In the creation ofpetrochemical-based leather alternatives (e.g., those based on PVC orPU), coatings may or may not be required, but when used, they aregenerally also petrochemical-based. In the development of anon-petrochemical and non-animal-based leather alternative, that is amaterial based entirely on plant-derived ingredients, it may also bedesired to provide a coating that provides additional surfaceprotection, coloration, and/or improved haptics to the non-petrochemicaland non-animal-based leather alternative.

Summary

Generally, an illustrative embodiment of a coating may be createdentirely from plant-derived ingredients. This coating may beparticularly well suited for use on leather-like materials created fromepoxidized natural rubber-based formulations but is not so limitedunless otherwise indicated in the following claims. The coating createdaccording to the present disclosure may be configured as substantiallythe reaction product between epoxidized vegetable oil and apolyfunctional naturally occurring acid (such as citric acid) as furtherdisclosed in U.S. Pat. No. 10,400,061. The coating has been found togreatly improve the haptics of the products thus coated.

Illustrative Embodiments and Detailed Description

Animal-based leather materials exhibit a haptic quality that isparticularly smooth to the touch, even for textured articles. It hasbeen found that the relationship between the dynamic coefficient offriction and static (or “breakaway”) coefficient of friction is key toquantifying this attribute. In generally, rubbery materials tend to havehigh grip, which may be reflected in both the actual values of thecoefficients of friction (static and dynamic), while the staticcoefficient of friction is generally significantly higher than thedynamic coefficient of friction.

Certain leather-like materials (which are substitutes for animal-basedleather) have been found to exhibit characteristic rubber-likecoefficient-of-friction values; especially when such materials areformulated with epoxidized natural rubber (ENR). Formulations based onENR with a 25% epoxidation level tend to have higher friction thanformulations based on ENR with a 50% epoxidation level. This isconsistent with polymer theory that correlates the glass transitiontemperature (T_(g)) with the coefficient of friction. That is, higherT_(g) results in lower coefficient of friction while lower T_(g) resultsin higher coefficient of friction. It has been documented that roughlyeach increased percentage change in epoxidation degree increases theT_(g) by one degree Celsius. The coefficient of friction effect ofchanges in T_(g) is due to the rate at which polymer chains canrearrange to engage the contacting surface. Unfortunately, many consumergoods require a material with a low T_(g) to prevent articles frombecoming stiff or brittle at reduced ambient temperatures (as may beencountered in the winter). Thus, the T_(g) of the material formulatedfor low temperature flexibility (based on ENR with lower epoxidationlevels) tends to make the material more grippy, which negatively impactsthe haptics of an article.

Therefore, it is desired to have an article construction that has a basematerial with a low T_(g) and a coating with a relatively higher T_(g)while the coating ought to retain enough flexibility to avoid crackingat low temperatures. Additionally, testing the coefficient of frictionin such a way that captures data consistent with what is observed withhuman hands is challenging. Generally, tests between animal-basedleather and stainless-steel sheets and between animal-based leather andsilicone sheets give data that does not correlate with the order ofmagnitude in coefficient of friction (COF) that a human hand woulddetect. In contrast, testing animal-based leather against aPTFE-coated-fiberglass baking sheet shows similar static and dynamiccoefficients of friction while also giving a relatively low absolutevalue that reflects the feeling of the human hand. Taking that same testmethod and applying it to materials produced according to variousmethods disclosed in U.S. Pat. No. 10,400,061 gives the data shown inTable 1.

TABLE 1 Test results for an animal-based leather and two leather-likematerials. Counter- Dynamic Static Test material surface COF COFResin-coated plant- PTFE Coated 0.15 0.59 based leather FiberglassUncoated plant-based PTFE Coated 0.44 0.46 leather based on ENRFiberglass Red Leather- PTFE Coated 0.17 0.17 Smooth Front Fiberglass

From Table 1 we see that animal-based leather has a low static anddynamic COF while an uncoated plant-based leather material based on ENRhas a relatively higher COF. In the first row we see data that coatingsuch material with resin that is a reaction product between epoxidizedsoybean oil (ESO) and citric acid (various illustrative embodiments ofwhich may be produced by methods disclosed in U.S. Pat. No. 10,400,061)lowers the dynamic COF to a value closer to animal-based leather. Thisresults in a haptic quality that is considerably improved when comparedto the uncoated ENR-based leather-like material.

Specifically, the coating used for resin-coated plant-based leather inTable 1 may be formulated by making a curative as disclosed in U.S. Pat.No. 10,400,061 and then mixing that curative with additional ESO to makea temperature-curable resin. In the first stage of curative manufacture,citric acid is dissolved in isopropyl alcohol, ethanol, or a combinationof acetone and alcohol-containing solvent. In the second stage ofcurative manufacture ESO or similar epoxy-containing plant-basedtriglyceride oil is added to the dissolved citric acid solution andallowed to react while simultaneously removing the miscibilizingsolvent. An illustrative curative formulation may use 50 parts of citricacid to 50 parts of ESO to 400 parts of miscibilizing solvent. After thecurative has been formed and the miscibilizing solvent evaporated, thenroughly 100 parts of curative is mixed with another 100 parts of ESO tomake the coating resin. Such coating resin may be further diluted withsolvent to make it easier to spray or spread. An example dilution foreasy spreading may entail mixing the resin with an equal mass ofisopropyl alcohol, ethanol, or acetone. Subsequently, the dilutionsolvent is allowed to evaporate, and the resin-coated substrate may beplaced into an oven or a heated press to complete the curing reactionbetween the curative and the epoxidized plant-based triglyceride oil. Inone illustrative embodiment, the coating resin may require 10 minutes tocure at 150° C. The texture of the coating resin may be determined bytextured release paper or textured silicone sheets to give the desiredappearance and haptics without limitation unless otherwise indicated inthe following claims.

Another illustrative embodiment of a coating configured according to themethods disclosed herein is comprised of a resin coating formulationthat may be produced based on the ratio of 100 parts of curative with100 parts of ESO, which may be further modified for easy application.Specifically, such mixture may be diluted with acetone, isopropylalcohol, or ethanol at a ratio of 1:1 (mixed resin:solvent) up to 1:20(mixed resin:solvent). Generally, any chemically suitable solvent havinga boil point from approximately 55 degrees Celsius to approximately 85degrees Celsius may be used with various illustrative embodiments of acoating without limitation unless otherwise indicated in the followingclaims. Thinner dilutions may enable easy spraying of thin coatingswhile thicker dilutions may be more appropriate for roll-coating. Inanother illustrative embodiment, it has been found that the inclusion ofa thickening polymer may aid in both the haptics of the cured film andin preventing the resin from squeezing out during the molding step. Suchthickening polymers may include, but are not limited to unless otherwiseindicated in the following claims, shellac, cellulose acetate, celluloseacetate phthalate, hydroxypropyl cellulose, and other naturallyoccurring or naturally derived polymers (without limitation unlessotherwise indicated in the following claims) that are soluble inacetone, isopropyl alcohol, ethanol, or other suitable solvent withoutlimitation unless otherwise indicated in the following claims.Generally, any thickener having the desired effect on the coating duringuse for its intended application may be used to create an illustrativeembodiment of the coating disclosed herein without limitation unlessotherwise indicated in the following claims.

Release additives such as waxes may be included in the resin coating toimprove haptics and help release from texture paper. In one illustrativeembodiment olive wax has been found to be particularly advantageous forsuch purposes. In other illustrative embodiments as disclosed herein,ultra-violet (UV) light stabilizing additives such as micro-TiO₂ ornano-TiO₂ may be added to improve the light stability of the coating andprotect the underlying material, without departure from spirit of thisdisclosure and without limitation unless otherwise indicated in thefollowing claims.

It has been found that curing said coating resin by molding it betweenan ENR-based rubber substrate as disclosed in U.S. Pat. No. 10,400,061and textured silicone or texture paper yields and appearance and hapticquality that are particularly well suited for consumer goods thatrequire low dynamic COF, low gloss, and a “dry” hand.

It is generally understood that the T_(g) of materials correlates to theCOF and the resin coating as disclosed herein has a T_(g) higher thanepoxidized natural rubber, even at the 50% epoxidation level.Furthermore, the resin coating may have a relatively higher crosslinkdensity and thus may exhibit less conformability to the human hand.These attributes may contribute to the preferred “hand” of the material.

Industrial Applicability

Various illustrative embodiments of resin coatings as disclosed hereinmay be particularly suited to coating ENR-based rubber substrates as maybe used in wallets, handbags, purses, shoes, belts, and similar consumeritems that may be normally made of leather or PU/PVC faux leatherwithout limitation unless otherwise indicated in the following claims.Illustrative embodiments of a coating disclosed herein may beparticularly advantageous in being used to coat ENR-based rubber becauseof the inherent material compatibility between coating and substrate.For example, and without limitation unless otherwise indicated in thefollowing claims, it has been found that thin coatings (e.g., less than200 microns) as applied using textured silicone or texture paper areflexible enough to withstand bending at −15° C. without delamination orcracking; whereas such coating materials when subject to bending at lowtemperatures as a bulk material (thickness greater than 500 microns) areprone to cracking.

Untextured oven-curing such coatings may result in a glossy surface thathas less desirable haptics when compared to press-cured and texturedcoatings. In some illustrative embodiments, the press-curing of thecoating may occur concurrently with the curing of the substrateENR-based rubber material. In other illustrative embodiments, thesubstrate may be cured in a first step, the coating applied in a secondstep, and the coating cured against textured silicone or texture paperin a third step.

In other illustrative embodiments, the resin coating may be applieddirectly to fabrics to provide water resistance. In such illustrativeembodiments, a higher dilution level of the coating solution (e.g.,˜3-6% solids) may yield a fabric with water resistance while retainingthe flexible hand of the fabric. Higher solids contents may yield morebarrier resistance with a stiffening of the substrate.

Materials made and/or coated according to any teaching of thisdisclosure may be used as flooring, exercise mats, bedding, shoeinsoles, shoe outsoles, or sound absorption panels without limitationunless otherwise indicated in the following claims.

Materials made and/or coated according to any teaching of thisdisclosure may be molded into complex three-dimensional articles andmulti-laminated articles. Three-dimensional articles may also consist ofmultiple material formulations arranged at various locations within anarticle to provide functionality required for each location.

The resilient memory foam based on vegetable oil may be used inapplications where polyurethane is used today. Such applications mayinclude shoes, seating, flooring, exercise mats, bedding, soundabsorption panels, and the like without limitation unless otherwiseindicated in the following claims. Many of these articles are consumableitems that if made from synthetic polyurethane foams arenon-biodegradable and are non-recyclable. If such items are made fromthe material disclosed herein, they would be biodegradable and thus notcreate a disposal problem.

Although the methods described and disclosed herein may be configured toutilize a coating comprised of a natural materials, the scope of thepresent disclosure, any discrete process step and/or parameterstherefor, and/or any apparatus for use therewith is not so limited andextends to any beneficial and/or advantageous use thereof withoutlimitation unless so indicated in the following claims.

3. Epoxidized Rubber

A. Summary

Coated fabrics prepared as disclosed in Section 2 above use a liquidusviscosity resin that allows such materials to flow into fabric andnon-woven substrates. The resulting cured materials have mechanicalproperties that reflect highly-branched structures with limited polymerflexibility between crosslinks (modest strength and modest elongation).One means of increasing the mechanical properties is to begin withpolymeric materials that have more linear structures and can be curedwith lower cross-link density. The incorporation of shellac resin (whichis a high molecular weight natural resin) in coated fabric recipes wasfound to improve strength and elongation but was also found to make thematerials more plastic. Material formulations as disclosed in Section3—Epoxidized Rubber are able to exhibit excellent mechanical properties(very high strength and higher elongation) without compromising materialflexibility at room temperature.

A natural material based on epoxidized natural rubber (ENR) is disclosedthat contains no animal-based substances and is substantially free ofpetrochemical-containing materials. In certain embodiments this naturalmaterial may serve as a leather-like material (which may be a substitutefor animal-hide leather and/or petrochemical-based leather-like products(e.g., PVC, polyurethane, etc.) without limitation unless otherwiseindicated in the following claims. Furthermore, the natural materialbased on ENR as disclosed herein may be configured to be substantiallyfree of allergens that may cause sensitivity in certain people. Thematerial disclosed herein is more cost effective and scalable than otherproposed materials for petrochemical-free vegan leather. With certaintreatments the natural material may also be made water resistant, heatresistant, and retain flexibility at low temperatures. This set ofbeneficial attributes may apply to any natural material based on ENRthat is produced according to the present disclosure and to whichadditional treatments are applied, as suitable to a particularapplication, as disclosed and discussed herein.

In at least one embodiment, an elastomeric material may be formed toinclude at least a primary polymeric material further comprised ofepoxidized natural rubber and a curative comprised of a reaction productbetween a polyfunctional carboxylic acid and an epoxidized vegetable oilas disclosed in Section 1—Curative. The elastomeric material may also beformed wherein the primary polymeric material is greater in volumetricproportion in comparison to the curative. The elastomeric material mayalso be formed to wherein the epoxidized natural rubber has a degree ofepoxidation between 3% and 50% without limitation unless otherwiseindicated in the following claims. Another embodiment of the elastomericmaterial may be comprised of a primary polymeric material comprised ofepoxidized natural rubber and a cure system that is not sulfur-based norperoxide-based, and wherein the cure system contains over 90% reactantsfrom biological sources.

In another embodiment, an article may be formed from the reactionproduct of epoxidized natural rubber and a curative wherein the curativeis the reaction product between a naturally occurring polyfunctionalcarboxylic acid and an epoxidized vegetable oil. In another embodiment,an article comprised of epoxidized natural rubber with fillers includingcork powder and precipitated silica may be formed and the article may bemolded as a sheet with leather-like texture. In another embodiment, anarticle may be formed wherein the reaction product further containsfillers of cork powder and silica. In another embodiment, the articlemay be formed or configured such that two or more layers of the reactionproduct have substantially different mechanical properties and themechanical property differences are due to differences in fillercomposition.

B. Illustrative Methods and Products

Epoxidized natural rubber (ENR) is a commercially available productunder the tradename Epoxyprene® (Sanyo Corp.). It is available in twogrades with 25% epoxidation and 50% epoxidation, ENR-25 and ENR-50respectively. However, in certain embodiments it is contemplated that anENR with a level of epoxidation between 3% and 50% may be used withoutlimitation unless otherwise indicated in the following claims. One ofordinary skill will appreciate that ENR may also be produced fromprotein denatured or removed latex starting products. During theepoxidation of natural rubber, it has been found that the allergenactivity is significantly reduced—the literature for Epoxyprenediscloses that the Latex Allergen Activity is only 2-4% of that ofuntreated natural rubber latex products. This is a substantialimprovement for those that may experience latex allergies. ENR is usedin materials of the present disclosure to impart elongation, strength,and low temperature flexibility to the products disclosed and claimed.

ENR is traditionally cured with chemistries that are common in therubber compound literature, e.g., sulfur cure systems, peroxide curesystems, and amine cure systems. According to the present disclosure, aspecially prepared curative with carboxylic acid functionality isprepared to be used as the curative as fully disclosed in Section 1above. There are a number of naturally-occurring polyfunctionalcarboxylic acid containing molecules, including but not limited tocitric acid, tartaric acid, succinic acid, malic acid, maleic acid, andfumaric acid. None of these molecules are miscible in ENR and thus havelimited effectivity and utility. It has also been found that a curativeof, for example, citric acid, and an epoxidized vegetable oil may beprepared that is soluble in ENR. Specifically, curatives of epoxidizedsoybean oil (ESO) and citric acid have been prepared with an excess ofcitric acid to prevent gelation of the ESO. Citric acid itself is notmiscible in ESO, but it has been advantageously been discovered thatsolvents such as isopropyl alcohol, ethanol, and acetone (for examplebut without limitation unless otherwise indicated in the followingclaims) may make a homogeneous solution of citric acid and ESO. In thissolution, the excess citric acid is made to react with the ESO andcreate a carboxylic-acid-capped oligomeric material (that is stillliquid) as shown in FIG. 1 . The miscibilizing solvent contains at leastsome hydroxyl-containing (i.e., alcohol) solvent that at least partiallyreacts with some of the carboxylic acid functional groups on the citricacid. The majority of the solvent is removed with elevated temperatureand/or vacuum—leaving behind a curative that may be used as a misciblecurative for the ENR. By thus constructing the curative, the resultantmaterial is substantially free of petrochemical-sourced inputs.

First Illustrative Embodiment and Process for the Creation of Curativethat is Used in the Preparation of ENR-Based Material

Curative was prepared by dissolving 50 parts of citric acid in a warmblend of 50 parts of isopropyl alcohol and 30 parts of acetone. Afterthe citric acid was dissolved, 15 parts of shellac flakes (blondedewaxed) were added to the mixture along with 50 parts of ESO. Themixture was heated and stirred continually until all the volatilesolvents had evaporated. It is noteworthy that the total residual volumeis greater than that of the citric acid, ESO, and shellac—meaning thatsome of the isopropyl alcohol (IPA) is grafted onto the citric acidcapped curative (via an ester linkage). Varying the ratio of IPA toacetone can vary the degree of IPA grafting onto the curative.

Second Illustrative Embodiment and Process for ENR-Based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 30 parts of the curative as prepared in the firstembodiment. In addition, 70 parts of ground cork powder (MF1 fromAmorim) was added as a filler. This mixture was made on a two-rollrubber mill according to normal compounding practices. The mixture wassheeted out and molded at 110° C. for 30 minutes. It was found to beproperly cured, with similar elongation and strain recovery as sulfurand peroxide cure systems.

Third Illustrative Embodiment and Process for ENR-Based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 45 parts of the curative as prepared in the firstembodiment. In addition, 70 parts of ground cork powder (MF1 fromAmorim) was added as a filler. This mixture was made on a two-rollrubber mill according to normal compounding practices. The mixture wassheeted out and molded at 110° C. for 30 minutes. It was found to befully cured, but with some attributes of over-crosslinked systems;including lower tear resistance and very high resilience.

Fourth Illustrative Embodiment and Process for ENR-based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 15 parts of the curative as prepared in the firstembodiment. In addition, 70 parts of ground cork powder (MF1 fromAmorim) was added as a filler. This mixture was made on a two-rollrubber mill according to normal compounding practices. The mixture wassheeted out and molded at 110° C. for 30 minutes. It was found to becured, but with a relatively low state-of-cure; with attributes such aslow resilience and poor strain recovery.

Fifth Illustrative Embodiment and Process for ENR-based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 30 parts of the curative as prepared in the firstembodiment. In addition, 70 parts of ground cork powder (MF1 fromAmorim) was added as a filler. Additionally, 20 parts of garneted fiber(from recovered textiles) was added. This mixture was made on a two-rollrubber mill according to normal compounding practices. The mixture wassheeted out and molded at 110° C. for 30 minutes. It was found to befully cured and additionally had a relatively high extensional modulusin accordance with the fiber content.

Sixth Illustrative Embodiment and Process for ENR-based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 30 parts of the curative as prepared in embodiment 1.In addition, 60 parts of ground cork powder (MF1 from Amorim) was addedas a filler. Additionally, 80 parts of garneted fiber (from recoveredtextiles) was added. This mixture was made on a two-roll rubber millaccording to normal compounding practices. The mixture was sheeted outand molded at 110° C. for 30 minutes. It was found to be fully cured andadditionally had a very high extensional modulus in accordance with thefiber content.

Seventh Illustrative Embodiment and Process for ENR-based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 60 parts of the curative as prepared in embodiment 1.In addition, 35 parts of ESO was added as a reactive plasticizer. Inaddition, 350 parts of ground cork powder (MF1 from Amorim) was added asa filler. Additionally, 30 parts of garneted fiber (from recoveredtextiles) was added. This mixture was made on a two-roll rubber millaccording to normal compounding practices. The mixture was sheeted outand molded at 110° C. for 30 minutes. It was found to be fully cured,rigid, and additionally had a relatively high extensional modulus inaccordance with the fiber content.

Eighth Illustrative Embodiment and Process for the Creation of Curativethat is Used in the Preparation of ENR-Based Material

Curative was prepared by dissolving 50 parts of citric acid in a warmblend of 110 parts of isopropyl alcohol. After the citric acid wasdissolved, 50 parts of ESO was added to the mixture along with 10 partsof Beeswax. The mixture was heated and stirred continually until all thevolatile solvents had evaporated. The total residual volume is greaterthan that of the citric acid, ESO, and beeswax—meaning that some of theisopropyl alcohol (IPA) is grafted onto the citric acid capped curative(via an ester linkage). The reduced liquid mixture was added to fineprecipitated silica (Ultrasil 7000 from Evonik) to make a 50 wt % dryliquid concentrate (DLC) for easy addition in subsequent processing.

Ninth Illustrative Embodiment and Process for ENR-Based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 50 parts of the curative DLC as prepared in theeighth illustrative embodiment along with 30 additional parts of fineprecipitated silica. It was found that mixing of the curative DLCprepared in eighth illustrative embodiment eliminated some stickiness inprocessing that was experienced when mixing in curative that was notpre-dispersed as a DLC. The resulting mixture was cured in a press at˜50 psi at 110° C. for 30 minutes to make a translucent slab.

The material of this embodiment was found to have attributes that areanalogous to those found in animal-hide leather; including slow recoveryafter folding, vibration damping attributes, and high tear strength. Itis believed that the total silica loading (55 parts) and this particularcurative contribute to the “lossy” characteristics of this material.Without wishing to be bound by theory, it is possible that the level oftotal silica loading is approaching the percolation threshold andcreating particle-particle interactions that are creating the lossyattributes without limitation unless otherwise indicated in thefollowing claims. This is a preferred mechanism to reliance on polymerformulations that experience a T_(g) near room temperature as a means tocreate a lossy material, as such an approach would lead to poor coldcrack resistance.

Tenth Illustrative Embodiment and Process for ENR-Based Material

Epoxidized Natural Rubber with 25% epoxidation (ENR-25) was mixed at 100parts of rubber to 30 parts of so-called “cottonized” hemp fiber, thismixture was mixed on a two-roll mill using a tight nip to get an evendispersion of fiber. To this masterbatch 50 parts of the curative DLC asprepared in the eighth illustrative embodiment along with 30 additionalparts of fine precipitated silica. The resulting mixture was cured in apress at ˜50 psi at 110° C. for 30 minutes to make a translucent slab.The material of the tenth illustrative embodiment was found to havesimilar attributes as the material of the ninth illustrative embodimentwith the change of having much lower elongation at break and much highermodulus in accordance with the fiber loading.

Eleventh Illustrative Embodiment and Process for ENR-Based Material

A black batch of ENR-based material was prepared by mixing ENR-25 withcoconut charcoal to achieve the desired black color. In addition to theblack colorant, other ingredients were added to yield a processiblebatch of rubber. Other ingredients may include clay, precipitatedsilica, additional epoxidized soybean oil, castor oil, essential oilodorants, tocopheryl (Vitamin E—as a natural antioxidant), and curative.This material was then cured in a tensile-plaque mold at 150° C. for 25minutes to complete the curing.

Twelfth Illustrative Embodiment and Process for ENR-Based Material

A brown batch of ENR-based material was prepared by mixing ENR-25 withcork powder to achieve the desired brown color and texture. In additionto the cork, other ingredients were added to yield a processible batchof rubber. Other ingredients may include clay, precipitated silica,additional epoxidized soybean oil, essential oil odorants, tocopheryl(Vitamin E—as a natural antioxidant), and pre-polymer curative. Thismaterial was then cured in a tensile-plaque mold at 150° C. for 25minutes to complete the curing.

Tensile stress-strain curves are shown in FIG. 9 for materials preparedaccording to the eleventh and twelfth embodiments. It can be seen thatthe cork-filled brown batch (twelfth embodiment) is higher in modulusthan the black batch (eleventh embodiment) for this particular example.In these two illustrative embodiments, the brown batch (twelfthembodiment) had a Shore A hardness of 86 while the black batch (eleventhembodiment) had a Shore A hardness of 79.

The optimal amount of the additional materials may vary according to thespecific application of the ENR-based material, and various ranges forsame are shown in Table 2.

TABLE 2 Acceptable and Preferred Ranges of Other Ingredients. PreferredRange Acceptable Range (Percent of Total (Percent of Total IngredientProduct Weight) Product Weight) ENR-25 40-60  20-90  Curative 2-10 1-50Cork 3-10 0-70 Colorant 0-15 0-50 Precipitated Silica 15-35  0-50 EVO0-10 0-30 Non-reactive vegetable oil 0-10 0-30 Odorant 0.5-3    0-10Vitamin E/antioxidant 0.2-2    0-4  Mineral filler (e.g., clay) 0-150-50

Variations in the other ingredients: clay, precipitated silica,additional epoxidized soybean oil, castor oil, and/or amount of curativemay be used to vary the modulus of a batch/recipe within a range that ischaracteristic of traditional rubber recipes. By those well versed inrubber compounding it is recognized that formulations of rubber may beselectively compounded with hardnesses ranging from approximately 50Shore A up to about 90 Shore A. The illustrative formulations show thatthese compounds fall within the range of expected performance forepoxidized natural rubber. Furthermore, it is known that traditionallycompounded natural rubber may achieve strength values from 10-25 MPa.The eleventh illustrative embodiment displays physical properties inline with traditionally compounded natural rubber.

Materials made according to this disclosure may further be reinforcedwith continuous fiber to make stronger products. Methods forreinforcement may include but are not limited to use of both woventextiles, non-woven textiles, unidirectional strands, and pliedunidirectional layers unless otherwise indicated in the followingclaims. Reinforcement may preferably come from natural fibers and yarns.Illustrative yarns may include, but are not limited to, cotton, jute,hemp, ramie, sisal, coconut fiber, kapok fiber, silk, or wool andcombinations thereof unless otherwise indicated in the following claims.Regenerated cellulose fibers such as viscose rayon, Modal® (a specifictype of viscose, by Lenzing), Lyocell (also known as Tencel®, byLenzing), or Cuprammonium Rayon may also be used without limitation orrestriction, as suitable for a particular application, unless otherwiseindicated in the following claims. Alternatively, reinforcement mayrequire the strength of synthetic fiber yarns based on para-aramids,meta-aramids, polybenzimidazole, polybenzoxazole, and similar highstrength fibers. In another illustrative embodiment, a reinforcementlayer and/or material may be configured from a protein-based fiber,which fibers include but are not limited to of wool, silk, alpaca fiber,qiviut, vicuna fiber, llama wool, cashmere, and angora unless otherwiseindicated in the following claims. Illustrative natural yarns maybeneficially be treated by the natural fiber welding process to improvetheir strength, reduce their cross-sectional diameter, and improvefiber-to-elastomer bonding characteristics. Such yarns may be plied intothreads that provide interpenetration features between reinforcement andelastomer as well as improve the strength of the reinforcement. Forcertain applications it may be preferred to provide reinforcement byunidirectional reinforcement in plied layers as compared to woven andknit reinforcement. It has been found that such woven and knitreinforcement may improve product stiffness but may negatively impacttear strength by creating stress-concentration features around yarns andfibers. In contrast, unidirectional reinforcement at various ply anglesmay avoid such stress concentrating features. In a related way,non-woven mats may be used as reinforcement as they do not containregularly oriented stress-concentrating features but do enable longreinforcement fiber lengths at high fiber volume fractions. In a relatedway, integrally mixed fiber content has been found to improve stiffnessbut decrease tear strength at certain volume and weight fractions. Tearstrength improvement is observed when total fiber content exceeds 50 phr(in traditional rubber compounding nomenclature), especially with evendispersion and good retention of fiber length during processing.

Molding and curing of materials according to the present disclosure hasbeen found to require only modest pressure to achieve porosity-freearticles. While traditional rubber cure systems evolve gasses and thusrequire molding pressures generally greater than 500 psi and oftencloser to 2000 psi, the compounds disclosed herein only require moldingpressure of 20 psi-100 psi, or more specifically 40 psi-80 psi toachieve consolidation and porosity-free articles. The actual requiredpressure may be dependent more on the amount of material flow and detailrequired in the final article. Such low molding pressures allow theusage of much lower tonnage presses that are correspondingly lessexpensive. Such pressures also allow much less expensive tooling; evenembossed texture papers have been found to create suitable patterns inelastomeric materials made according to this disclosure and such texturepapers are found to be reusable for multiple cycles without loss ofpattern detail. The material edge strength has been found to be adequateeven when using open-sided tooling—this allows for faster tool cleaningand significantly reduced tooling costs.

The low molding pressures further allow for such elastomeric materialsto be molded directly onto the surface of resilient and porous coresubstrates. For example, the material may be overmolded onto non-woveninsulative mats as a resilient flooring product or automotive interiorproduct that exhibits soft-touch and sound absorption characteristics.Similarly, the product may be overmolded onto softwoods or similar lowcompressive strength substrates without damage to the substrate.

As previously described, certain catalysts are known in the art to speedup the carboxylic acid addition to epoxide groups and such may be usedin formulating recipes according to the present disclosure withoutlimitation unless otherwise indicated in the following claims.

Animal-hide leather has distinctive characteristics in terms ofelongation, resiliency, loss modulus, and stiffness that are differentthan a regularly compounded elastomer. In particular, animal-hideleather may be folded back on itself without cracking—largelyindependent of temperature. That is, it does not have a material phasethat becomes brittle at low temperatures. Animal-hide leather also hasvibration damping characteristics that are less common with regularlycompounded elastomeric compounds. Animal-hide leather has slow recoveryafter creasing or folding, but does generally recover completely withminimal plastic deformation. These attributes may be mimicked inmaterials compounded according to the present disclosure in theillustrative embodiments and methods for same disclosed herein.

C. Additional Treatments

Articles produced according to this disclosure may be finished by anymeans known in the art. Such means include but are not limited toembossing, branding, sanding, abrading, polishing, calendering,varnishing, waxing, dyeing, pigmenting, and the like unless otherwiseindicated in the following claims. Such articles may be configured toexhibit characteristics very analogous to animal-hide leather. Thesurfaces then may be treated with natural oil or wax protectants,subject to a particular application.

D. Applications/Additional Illustrative Products

Articles molded with materials according to this disclosure may be usedas plant-based alternatives to petrochemical-based leather-like productsand/or animal-hide leather products. In one illustrative embodiment thearticles may be molded substantially as sheets with various texturesaccording to the desired application. The sheets may be used in durablegoods such as upholstery, seating, belts, shoes, handbags, purses,backpacks, straps, equestrian gear, wallets, cellular phone cases, andsimilar articles without limitation unless otherwise indicated in thefollowing claims. Alternatively, such materials may be molded directlyto the shape of the final article in applications such as shoe soles,shoe toes, shoe heal cups, shoe uppers, purses, horse saddles and saddlecomponents, helmet coverings, chair armrests, and similar articles.

Materials according to this disclosure may be overmolded onto resilientmaterials and thus be used as flooring, exercise mats, or soundabsorption panels. Similarly, those materials could be overmolded ontogarments as, for example, a knee patch or elbow patch for improvedabrasion resistance for a region of a garment. Likewise, motorcyclegarments (e.g., chaps) and equestrian gear may be overmolded ofmaterials according to this disclosure to provide improved localabrasion resistance and protection.

Materials according to this disclosure may be molded into complexthree-dimensional articles and multi-laminated articles. That is,certain formulations according to this disclosure may provide improvedtear strength, while other formulations according to this disclosure mayprovide improved abrasion resistance. Such formulations may be laminatedand co-molded to provide articles with improved overall performancecompared with an article made of only one formulation. Three-dimensionalarticles may be molded to provide additional product features,attachment points, and other functionality without limitation unlessotherwise indicated in the following claims. Three-dimensional articlesmay also consist of multiple formulations arranged at various locationswithin an article to provide functionality required for each location.

One example of such molded-in functionality is shown in FIGS. 10A & 10B,which provides a perspective view of a portion of a belt made of anENR-based material. Specifically, in FIG. 10A, a tapered feature (shownon the right-hand side of FIG. 10A) may be molded into a sheet that islater slit into belt sections. The reduced thickness (which may be dueto the absence of a backing material/backing layer (e.g., non-woven mat)in the area having reduced thickness) allows for a folded buckleretention area that is substantially similar in thickness to beltsections that are not folded over on itself, which is shown in FIG. 10Bwhere the reduced-thickness area has been engaged with a buckle.Additionally, the region that is folded back onto itself may bepreferentially bonded in place with additional resin or ENR-basedmaterial molded between the folded region with a cure cycle that issimilar to that used during the initial molding of the sheet.

Shown in FIG. 11 are a series of retention grooves and ridges that maybe molded into the end of the belt to provide a friction-based retentionfeature. That is, some belts made with woven nylon or other textiles aretightened and retained on the wearer by friction between ribs woven intothe belt and a metal bar used in the clasp. Such features may beadvantageous in that they prevent stress risers from developing aroundpunched holes used for retention in common belt buckles. Retentiongrooves & ridges and/or other features for retaining the position of aportion of a belt easily molded into a belt sheet by the creation ofmatching features in the mold tooling (which may be silicone or metal)when making an ENR-based material according to the present disclosure.

ENR-based materials configured for use as a belt may be made in sheetsand may be produced by molding according to the pattern illustrated inFIG. 12 . As shown in FIG. 12 , the sheet may be comprised of variouslayers, wherein each outside layer of the sheet may be comprised of anENR-based material (e.g., “sheeted rubber preform” in FIG. 12 ) with oneor more fibrous backing materials/backing layers positionedtherebetween. The backing materials may be comprised of a wovenreinforcement or a non-woven mat in the illustrative embodiment shown inFIG. 12 , but any suitable backing material/backing layer may be usedwithout limitation unless otherwise indicated in the following claims.At least one of the backing materials may be a coated fabric (as shownin FIG. 12 for the layer labeled “non-woven mat”), which may beconstructed in accordance with Section 2 described herein above. Texturepaper may be positioned adjacent one or both ENR-based material layersto provide the desired aesthetics to the outer layers of the sheet andresulting article. Finally, a silicone release sheet may be positionedadjacent one or both texture papers for ease of use.

It has been found that the relatively low required pressure to yield aproperly cured specimen utilizing ENR-based materials allows for the useof low-cost paper and silicone tooling. So-called texture papers areused in polyurethane and vinyl leather alternatives to achieve thedesired texture. It has been found that these texture papers likewiseare effective in creating patterns in ENR-based materials as disclosedherein. An advantageous molding configuration is shown in FIG. 12 ,wherein release silicone sheets are provided as the top-most andbottom-most layers in the sandwich that is molded under temperature andpressure. If the “outside” faces of the belt are desired to be textured,texture paper may be provided next to the silicone sheets. These mayadvantageously be treated with a release aid to promote easy release andreuse of the texture paper. Silicone and vegetable oil have both beenfound to be effective in release and reuse of the texture paper but anysuitable release agent may be used without limitation unless otherwiseindicated in the following claims.

The uncured rubber pre-form sheets may be loaded into the sandwich nextto the texture paper(s). Between the rubber pre-form sheets a non-wovenmat and/or woven reinforcement layer(s) may be provided. In oneillustrative embodiment, the non-woven mat may comprise recycledtextiles, hemp fibers, coconut coir fibers, or other environmentallybenign (biodegradable) fibers, and/or combinations thereof withoutlimitation unless otherwise indicated in the following claims. In oneillustrative embodiment the woven reinforcement layer may comprise juteburlap or similar open-structure woven product that is high in strengthand biodegradable. In another illustrative embodiment so-called cottonmonk's cloth may be also used as a woven reinforcement layer withoutrestriction unless otherwise indicated in the following claims. In someconfigurations open-structure woven products provide relatively goodtear strength when compared to tight woven fabrics. In anotherillustrative embodiment, a reinforcement layer (woven or non-woven) maybe configured from a protein-based fiber, which fibers include but arenot limited to of wool, silk, alpaca fiber, qiviut, vicuna fiber, llamawool, cashmere, and angora unless otherwise indicated in the followingclaims.

ENR-based materials configured for use as leather substitutes may beused in applications where animal-hide leather is used today. Suchapplications may include belts, purses, backpacks, shoes, table tops,seating, and the like without limitation unless otherwise indicated inthe following claims. Many of these articles are consumable items thatif made from petrochemical-based leather-like products arenon-biodegradable and are non-recyclable. If such items are made fromthe material disclosed herein, they would be biodegradable and thus notcreate a disposal problem. Furthermore, unlike animal-hide leather,which requires significant processing to be made durable and stable(some of which uses toxic chemicals), the materials disclosed herein mayrequire less processing and will use environmentally friendly chemicals.Additionally, animal-hide leather is limited in size and may containdefects that render large pieces inefficient to produce. The materialdisclosed in at least one embodiment herein does not have the same kindof size limitations as the reaction between epoxide groups andcarboxylic groups does not create any condensation by-products, there isno inherent limit to the cross-sectional thickness that may be created.

4. Foam Material

A. Background

Most resilient foam products that are commercially available are basedon synthetic polymers, specifically polyurethane. A key attribute thatdifferentiates so-called memory foam from other foam products is theglass transition temperature (T_(g)) of the polymer. Rigid foams aregenerally comprised of polymers with a T_(g) well above roomtemperature, an illustrative example of such a product is polystyrenefoam (often used in rigid insulation boards and insulated drinkingcups). Flexible and springy foams are generally comprised of polymerswith a T_(g) well below room temperature, an exemplary example of such aproduct is a car door weather seal based on ethylene-propylene rubber(EPR/EPDM). Natural products may be likewise found in both rigid andflexible/springy categories. Balsa wood is a generally porous andfoam-like material that is substantially rigid at room temperature.Natural rubber latex may be foamed by either the Talalay or Dunlopprocess to make a flexible and springy foam product that issubstantially comprised of naturally-occurring polymers. To date, thereis no widespread naturally occurring foam that has a T_(g) near roomtemperature to yield a lossy foam that is the key attribute of memoryfoam materials.

Natural materials that make flexible foam products today are often basedon natural rubber latex. To make latex products stable to temperatureexcursions, the polymer must be vulcanized (i.e., crosslinked).Vulcanization of natural rubber may occur through a few known methods;most often sulfur vulcanization may be used, but peroxide or phenoliccure systems may likewise be used. Although sulfur and zinc oxide curesystems may be capable of vulcanizing natural rubber latex, very oftenother chemicals are added to increase the cure rate, limit reversion,and provide other functional benefits (e.g., anti-oxidants,anti-ozonates, and/or UV stabilizers). These additional chemicals maycreate chemical sensitivities in certain individuals. Also, naturalrubber latex itself may cause allergic reactions in certain individualsdue to the natural proteins that exist in the latex.

Similar natural rubber latex formulations may likewise be used as a gluefor fibrous mats to create a resilient foam-like product. Notably,coconut fiber may be bonded together by natural rubber latex into anon-woven mat to provide a cushion or mattress material that issubstantially all-natural in origin. Despite various claims in the priorart of being “all natural,” the cure system and additives to the naturalrubber may contain synthetic chemicals that may create chemicalsensitivities in certain individuals; furthermore, the natural rubberlatex itself may cause allergic reactions in certain individuals due tothe residual protein.

B. Summary

A foam product based on epoxidized vegetable oil is disclosed whereinthe pre-polymer curative is likewise comprised of naturally occurringand naturally derived products of biological origin. The foam productdisclosed is created without the use of additional foaming agent. Thefoamed product may be created with or without the requirement ofwhipping in air into the pre-cured liquid resin. The foam productdisclosed may have a T_(g) near room temperature, thus providing a lossyproduct. Additionally, the foam product may be formulated to have aT_(g) below room temperature to provide a flexible, springy product.Memory foam attributes may be attained by polymers prepared according tothis disclosure. Such polymers are reaction products of the pre-polymercurative as described herein above and epoxidized vegetable oils,reaction mixtures may also contain other natural polymers and modifiednatural polymers as described in further detail below.

In certain embodiments, the foam product may contain a certain fractionof epoxidized natural rubber. Notably, the process that createsepoxidized natural rubber also reduces the free protein that may createallergic reactions in certain individuals. The reduction in allergicresponse for epoxidized natural rubber compared to untreated naturalrubber is greater than 95%.

Disclosed is a castable resin comprising EVO (and/or any suitableepoxidized triglyceride as disclosed above) combined with thepre-polymer curative (as disclosed above in Section 1), and in oneillustrative embodiment ENR that has been solubilized in the EVO.

It has been found that a pre-polymer curative, as disclosed in Section1, can be created that eliminates the risk of porosity when cured withina certain temperature range, but that evolves gas during the curingprocess when conducted within a second higher temperature range.Furthermore, the oligomeric pre-polymer curative may incorporatesubstantially all of the polyfunctional carboxylic acid so that noadditional solvent is required during the curing process. For example,citric acid is not miscible in ESO but they may be made to react witheach other in a suitable solvent. The amount of citric acid may beselected so that the pre-polymer curative is created so thatsubstantially all of the epoxide groups of the ESO in the pre-polymercurative are reacted with carboxylic acid groups of the citric acid.With sufficiently excess citric acid, the pre-polymerization extent maybe limited so that no gel fraction is formed. That is, the targetpre-polymer curative is a low molecular weight (oligomeric) citric-acidcapped ester-product formed by the reaction between carboxylic acidgroups on the citric acid with epoxide groups on the ESO.

Illustrative oligomeric pre-polymer curatives may be created with weightratios of ESO to citric acid in the range of 1.5:1-0.5:1. If too muchESO is added during pre-polymer curative creation, the solution may geland further incorporation of ESO to create the target resin becomesimpossible. Note that on a weight basis, stoichiometric equivalentamounts of epoxide groups on the ESO and carboxylic acid groups on thecitric acid occur at a weight ratio of 100 parts of ESO to about 30parts of citric acid. A ratio of ESO:citric acid above 1.5:1 may build apre-polymer curative with excessive molecular weight (and henceviscosity) which limits its usefulness as a casting resin. If the ratioof ESO:citric acid is below 0.5:1 it has been found that there is somuch excess citric acid that after solvent evaporation, ungrafted citricacid may precipitate out of solution.

In addition to controlling the ratio of ESO to citric acid, according tothe present disclosure it has been found that selective control of theamount of alcohol used as a solvent may also be used to tailor thephysical properties of the resulting elastomeric foam. It has been foundthat the alcohol solvent may itself be incorporated into the elastomerby forming ester linkages with the polyfunctional carboxylic acid thatare reversible and thus gas-evolving when the material is cured at atemperature higher than that required to make a porosity-free product. Amixture of two or more solvents may be used to tailor the amount ofgrafting of an alcohol-containing solvent onto the citric acid-cappedoligomeric pre-polymer curative.

For example, and without restriction or limitation unless otherwiseindicated in the following claims, isopropyl alcohol (IPA) or ethanolmay be used as a component of a solvent system used to miscibilizecitric acid with ESO. IPA or ethanol are capable of forming an esterlinkage via a condensation reaction with citric acid. Since citric acidhas three carboxylic acids, such grafting reduces the averagefunctionality of the citric acid molecules that are reacting with theESO. This is beneficial in creating an oligomeric structure that is morelinear and therefore less highly branched. Acetone may be used as onecomponent of a solvent system used to miscibilize citric acid with ESO,but unlike IPA or ethanol, acetone itself is not capable of beinggrafted onto the citric acid-capped oligomeric pre-polymer curative.Indeed, during creation of the oligomeric pre-polymer curative it hasbeen found that the reactivity of the pre-polymer curative isdetermined, in part, by the ratio of IPA or ethanol to acetone that maybe used to solubilize citric acid with ESO. That is, in reactionmixtures with the similar amounts of citric acid and ESO, a pre-polymercurative created from a solution with a relatively high ratio of IPA orethanol to acetone creates a lower viscosity product than pre-polymercurative created from a solution with a relatively low ratio of IPA orethanol to acetone under similar reaction conditions. Also, the amountof IPA or ethanol grafted on the pre-polymer curative determines theextent to which such IPA or ethanol is evolved when the formulated resinis foamed at a temperature higher than that required to make aporosity-free resin product.

C. Illustrative Methods and Products

Illustrative blends that create resilient memory foams have been createdfrom a combination of inputs that include a pre-polymer curative, aliquid blend of epoxidized natural rubber and epoxidized vegetable oiland may contain unmodified epoxidized vegetable oil.

In a first illustrative embodiment of a foam material, the resilientmemory foam is produced using a pre-polymer curative creation and bydissolving 50 parts of citric acid in 125 parts of warm IPA, acceleratedby mixing (again with reference to FIG. 1 ). After dissolution of thecitric acid, 50 parts of ESO is added to the stirring solution. Thesolution is preferably mixed and reacted at temperatures of 60° C.-140°C. with optional use of mild vacuum (50-300 Torr). One illustrativebatch was mixed in a jacketed reactor vessel with a jacket temperatureof 120° C. (solution temperatures of ˜70° C.-85° C.) and the citric acidgrafting onto ESO occurred concurrently with IPA evaporation. At the endof the reaction sequence it was discovered that roughly 12 parts of IPAwas grafted onto the combined 100 parts of ESO and citric acid.Accordingly, temperatures above the boiling point of IPA and applicationof vacuum could no longer yield IPA condensate in the condensing system.Calculations reveal that of the starting carboxylic acid sites on thecitric acid, roughly 31% reacted with epoxide groups on the ESO(assuming all of the epoxides were converted during the reaction toester linkages), roughly 27% of the carboxylic acid sites reacted withIPA to form pendant esters, and roughly 42% remain unreacted andavailable for crosslinking the resin in a subsequent processing step.However, these calculations are for illustrative purposes only and in noway limit the scope of the present disclosure unless otherwise indicatedin the following claims.

In a second illustrative embodiment of a foam material, the resilientmemory foam was created via a rubber-containing resin precursor.Epoxidized natural rubber may be included in resin-based formulations atlevels below twenty-five weight percent (25 wt %) and still yield apourable liquid. Creation of the rubber-containing precursor may be donein two-stages without requiring the use of a solvent for rubberdissolution. In the first stage 100 parts of epoxidized natural rubber(ENR-25) are mixed with 50 parts of ESO using rubber mixing techniques(a two-roll mill or internal mixer). This yields a very soft gum thatcannot effectively be further mixed on rubber processing equipment, butwith the application of heat (e.g., 80° C.) additional ESO may be mixedinto the rubber with a Flacktek Speedmixer or alternative low-horsepowerequipment (e.g., a sigma-blade mixer) to create a flowable liquidcontaining 25% ENR-25 and 75% ESO.

A third illustrative embodiment of a foam material may also produce aresilient memory foam-type creation. In this embodiment, the foamableresin is produced via mixing and curing. For this illustrativeembodiment, 40 parts of pre-polymer curative from the first illustrativeembodiment of a foam material was added to 80 parts of rubber-containingresin from the second illustrative embodiment. The resulting combinationwas then mixed with a Flacktek Speedmixer until a homogeneous solutionwas obtained (about 10 minutes of mixing). This resin was cured usingthe following two procedures:

-   -   1. Resin cured on 200° C. (nominal temperature) hot griddle        (PTFE coated) just like a pancake. The material foamed to a        relatively homogenous article with memory-foam characteristics;        specifically, lossy behavior. A depiction of the resulting        material is shown in FIG. 13 .    -   2. Resin was vacuum degassed after mixing and placed on the same        200° C. hot griddle. In this instance, porosity was observed        over the heating element (measured temperature 210° C.) but no        porosity was observed over the region of the griddle without the        heating element (measured temperature 180° C.). Depictions of        the resulting materials are shown in FIG. 14 .

From these two procedures, it is clear that there may be two sources ofporosity. One source may involve small bubbles of air that areincorporated during mixing. Additional experimentation has shown thatthe presence of ENR-25 in the resin is an important contributor tostabilizing this incorporated air and preventing bubble coalescenceduring the curing stage. The second source of porosity is evolved gas,likely removal of the grafted IPA, at temperatures at or above 200° C.

As previously described, certain catalysts are known in the art to speedup the carboxylic acid addition to epoxide groups and such may be usedin formulating recipes according to the present disclosure withoutlimitation unless otherwise indicated in the following claims.

D. Applications/Additional Illustrative Products

Materials according to this disclosure may be used as flooring, exercisemats, bedding, shoe insoles, shoe outsoles, or sound absorption panelswithout limitation unless otherwise indicated in the following claims.

Materials according to this disclosure may be molded into complexthree-dimensional articles and multi-laminated articles.Three-dimensional articles may also consist of multiple materialformulations arranged at various locations within an article to providefunctionality required for each location.

The resilient memory foam based on vegetable oil may be used inapplications where polyurethane is used today. Such applications mayinclude shoes, seating, flooring, exercise mats, bedding, soundabsorption panels, and the like without limitation unless otherwiseindicated in the following claims. Many of these articles are consumableitems that if made from synthetic polyurethane foams arenon-biodegradable and are non-recyclable. If such items are made fromthe material disclosed herein, they would be biodegradable and thus notcreate a disposal problem.

Although the methods described and disclosed herein may be configured toutilize a curative comprised of a natural materials, the scope of thepresent disclosure, any discrete process step and/or parameterstherefor, and/or any apparatus for use therewith is not so limited andextends to any beneficial and/or advantageous use thereof withoutlimitation unless so indicated in the following claims.

The materials used to construct the apparatuses and/or componentsthereof for a specific process will vary depending on the specificapplication thereof, but it is contemplated that polymers, syntheticmaterials, metals, metal alloys, natural materials, and/or combinationsthereof may be especially useful in some applications. Accordingly, theabove-referenced elements may be constructed of any material known tothose skilled in the art or later developed, which material isappropriate for the specific application of the present disclosurewithout departing from the spirit and scope of the present disclosureunless so indicated in the following claims.

Having described preferred aspects of the various processes,apparatuses, and products made thereby, other features of the presentdisclosure will undoubtedly occur to those versed in the art, as willnumerous modifications and alterations in the embodiments and/or aspectsas illustrated herein, all of which may be achieved without departingfrom the spirit and scope of the present disclosure. Accordingly, themethods and embodiments pictured and described herein are forillustrative purposes only, and the scope of the present disclosureextends to all processes, apparatuses, and/or structures for providingthe various benefits and/or features of the present disclosure unless soindicated in the following claims.

While the chemical process, process steps, components thereof,apparatuses therefor, products made thereby, and impregnated substratesaccording to the present disclosure have been described in connectionwith preferred aspects and specific examples, it is not intended thatthe scope be limited to the particular embodiments and/or aspects setforth, as the embodiments and/or aspects herein are intended in allrespects to be illustrative rather than restrictive. Accordingly, theprocesses and embodiments pictured and described herein are no waylimiting to the scope of the present disclosure unless so stated in thefollowing claims.

Although several figures are drawn to accurate scale, any dimensionsprovided herein are for illustrative purposes only and in no way limitthe scope of the present disclosure unless so indicated in the followingclaims. It should be noted that the welding processes, apparatusesand/or equipment therefor, and/or impregnated and reacted uponsubstrates produced thereby are not limited to the specific embodimentspictured and described herein, but rather the scope of the inventivefeatures according to the present disclosure is defined by the claimsherein. Modifications and alterations from the described embodimentswill occur to those skilled in the art without departure from the spiritand scope of the present disclosure.

Any of the various features, components, functionalities, advantages,aspects, configurations, process steps, process parameters, etc. of achemical process, a process step, a substrate, and/or a impregnated andreacted substrate, may be used alone or in combination with one anotherdepending on the compatibility of the features, components,functionalities, advantages, aspects, configurations, process steps,process parameters, etc. Accordingly, an infinite number of variationsof the present disclosure exist. Modifications and/or substitutions ofone feature, component, functionality, aspect, configuration, processstep, process parameter, etc. for another in no way limit the scope ofthe present disclosure unless so indicated in the following claims.

It is understood that the present disclosure extends to all alternativecombinations of one or more of the individual features mentioned,evident from the text and/or drawings, and/or inherently disclosed. Allof these different combinations constitute various alternative aspectsof the present disclosure and/or components thereof. The embodimentsdescribed herein explain the best modes known for practicing theapparatuses, methods, and/or components disclosed herein and will enableothers skilled in the art to utilize the same. The claims are to beconstrued to include alternative embodiments to the extent permitted bythe prior art.

Unless otherwise expressly stated in the claims, it is in no wayintended that any process or method set forth herein be construed asrequiring that its steps be performed in a specific order. Accordingly,where a method claim does not actually recite an order to be followed byits steps or it is not otherwise specifically stated in the claims ordescriptions that the steps are to be limited to a specific order, it isno way intended that an order be inferred, in any respect. This holdsfor any possible non-express basis for interpretation, including but notlimited to: matters of logic with respect to arrangement of steps oroperational flow; plain meaning derived from grammatical organization orpunctuation; the number or type of embodiments described in thespecification.

What is claimed is:
 1. An article comprising: a. a substrate comprisedof a natural fiber; b. a coating engaged with said substrate, whereinsaid coating comprises a reaction product between a naturally occurringpolyfunctional carboxylic acid and an epoxidized triglyceride.
 2. Thearticle according to claim 1 wherein said coating further comprises athickener of naturally occurring or naturally derived polymer.
 3. Thearticle according to claim 1 wherein said thickener is further definedas being soluble in a solvent.
 4. The article according to claim 3wherein said solvent is further defined as being selected from a groupconsisting of acetone, isopropyl alcohol, and ethanol.
 5. The articleaccording to claim 1 wherein said thickener is further defined as beingselected from a group consisting of shellac, cellulose acetate,cellulose acetate phthalate, hydroxypropyl methylcellulose, andhydroxypropyl cellulose.
 6. The article according to claim 1 whereinsaid reaction product between said naturally occurring polyfunctionalcarboxylic acid and said epoxidized triglyceride further defined asbeing completed in a first stage and a second stage.
 7. The articleaccording to claim 6 wherein said first stage is further defined as saidnaturally occurring polyfunctional carboxylic acid being reacted withsaid epoxidized triglyceride in stoichiometric excess to form a firstmaterial, and wherein said second stage is further defined as combiningsaid first material with an additional portion of epoxidizedtriglyceride to create a thermoset resin coating.
 8. The articleaccording to claim 1 wherein said reaction product is further defined asincluding a formed ester linkage.
 9. The article according to claim 8wherein said reaction product is further defined as being among saidnaturally occurring polyfunctional carboxylic acid, said epoxidizedtriglyceride, and a hydroxyl-containing solvent.
 10. The articleaccording to claim 9 wherein said ester linkage is further defined asbeing formed between said hydroxyl-containing solvent and said naturallyoccurring polyfunctional carboxylic acid.
 11. A method for making acoating, said method comprising the steps of: a. mixing a naturallyoccurring polyfunctional carboxylic acid with an epoxidizedtriglyceride; and b. allowing said naturally occurring polyfunctionalcarboxylic acid and said epoxidized triglyceride to form an esterlinkage.
 12. The method according to claim 11 further comprising thestep of adding a thickener.
 13. The method according to claim 11 whereinsaid thickener is further defined as being soluble in a solvent.
 14. Themethod according to claim 13 wherein said solvent is further defined asbeing selected from a group consisting of acetone, isopropyl alcohol,and ethanol.
 15. The method according to claim 12 wherein said thickeneris further defined as being selected from a group consisting of shellac,cellulose acetate, cellulose acetate phthalate, hydroxypropylmethylcellulose, and hydroxypropyl cellulose.
 16. The method accordingto claim 11 wherein said reaction product between said naturallyoccurring polyfunctional carboxylic acid and said epoxidizedtriglyceride further defined as being completed in a first stage and asecond stage.
 17. The method according to claim 16 wherein said firststage is further defined as said naturally occurring polyfunctionalcarboxylic acid being reacted with said epoxidized triglyceride instoichiometric excess to form a first material, and wherein said secondstage is further defined as combining said first material with anadditional portion of epoxidized triglyceride to create a thermosetresin coating.
 18. The method according to claim 11 wherein saidreaction product is further defined as including a formed ester linkage.19. The method according to claim 18 wherein said reaction product isfurther defined as being among said naturally occurring polyfunctionalcarboxylic acid, said epoxidized triglyceride, and a hydroxyl-containingsolvent.
 20. The method according to claim 18 wherein said ester linkageis further defined as being formed between said hydroxyl-containingsolvent and said naturally occurring polyfunctional carboxylic acid.